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For Companies At a Glance
- Tasks: Join our team to monitor clinical sites and ensure compliance with regulations.
- Company: IQVIA is a global leader in clinical research, driving healthcare innovation.
- Benefits: Enjoy career development, innovative tools, and a supportive work environment.
- Why this job: Be at the forefront of medicine development and make a real impact on patient health.
- Qualifications: A life science degree and experience in site monitoring are essential.
- Other info: This role does not offer UK visa sponsorship.
The predicted salary is between 36000 - 60000 £ per year.
Our Sponsor Dedicated (cFSP) team is growing, and we are looking for aspiring CRAs of all levels to join us on our mission to drive healthcare forward!
What We Offer
- The chance to work on cutting-edge medicines at the forefront of new medicines development.
- Access to significant data pools through IQVIA, enabling better site selection and recruitment, which makes the CRA role more efficient and discussions at sites more productive.
- Next-generation clinical development!
- Genuine career development opportunities for those who want to grow within the organization.
- Investment in team stability to ensure a consistent workload.
- Provision of an iPad and access to innovative tools such as site visit apps and report apps to enhance efficiency.
Responsibilities
- Perform site monitoring visits (selection, initiation, monitoring, and close-out) in accordance with the scope of work and regulatory requirements, including GCP and ICH guidelines.
- Work with sites to develop, drive, and track subject recruitment plans aligned with project needs to improve predictability.
- Administer protocol and related study training to sites and establish regular communication to manage expectations and issues.
- Evaluate the quality and integrity of site practices, ensuring proper conduct of the protocol and adherence to regulations, escalating issues as needed.
- Manage study progress by tracking regulatory submissions, approvals, recruitment, CRF completion, data queries, and resolutions.
- Support start-up phase if applicable.
- Ensure site documents are properly filed in the Trial Master File (TMF) and maintain the Investigator's Site File (ISF) according to GCP and regulatory standards.
- Create and maintain documentation on site management, monitoring findings, and action plans, including visit reports and follow-up correspondence.
- Collaborate with study team members to support project execution.
- If applicable, support the development of site-specific recruitment plans and manage site finances according to trial agreements.
Requirements
- Life science degree or equivalent qualification.
- Experience in independent on-site monitoring.
- Experience managing multiple protocols and sites across various drug indications.
- Flexibility and willingness to travel.
- Strong communication, written, and presentation skills.
This role is not eligible for UK visa sponsorship. IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments, aiming to improve patient outcomes and population health worldwide. We value diverse talent with curious minds and a commitment to innovation. Everyone at IQVIA contributes to our shared goal of improving lives through healthcare. Thank you for your interest in growing your career with us.
Experienced Clinical Research Associate, Sponsor Dedicated employer: Nanosep AB
Contact Detail:
Nanosep AB Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Experienced Clinical Research Associate, Sponsor Dedicated
✨Tip Number 1
Familiarise yourself with the latest GCP and ICH guidelines, as these are crucial for a Clinical Research Associate role. Being well-versed in these regulations will not only boost your confidence but also demonstrate your commitment to compliance during interviews.
✨Tip Number 2
Network with current or former Clinical Research Associates to gain insights into their experiences and the challenges they face. This can provide you with valuable information that you can use to tailor your discussions during the interview process.
✨Tip Number 3
Showcase your flexibility and willingness to travel by sharing relevant experiences where you successfully managed multiple sites or protocols. Highlighting your adaptability can set you apart from other candidates.
✨Tip Number 4
Prepare specific examples of how you've improved site recruitment or managed study progress in previous roles. Concrete examples will help illustrate your problem-solving skills and effectiveness in a CRA position.
We think you need these skills to ace Experienced Clinical Research Associate, Sponsor Dedicated
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical research, particularly any roles where you've performed site monitoring visits or managed multiple protocols. Use keywords from the job description to align your skills with what the company is looking for.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your understanding of the role. Mention specific experiences that demonstrate your ability to drive subject recruitment plans and manage site communications effectively.
Highlight Relevant Qualifications: Clearly state your life science degree or equivalent qualifications in your application. If you have certifications related to Good Clinical Practice (GCP) or ICH guidelines, be sure to include those as well.
Showcase Communication Skills: Since strong communication skills are essential for this role, provide examples in your application of how you've successfully communicated with stakeholders in previous positions. This could include managing expectations, resolving issues, or presenting findings.
How to prepare for a job interview at Nanosep AB
✨Know Your Regulations
Familiarise yourself with GCP and ICH guidelines, as these are crucial in the role of a Clinical Research Associate. Being able to discuss how you have applied these regulations in past experiences will demonstrate your competence and understanding of the industry.
✨Showcase Your Communication Skills
As a CRA, strong communication is key. Prepare examples of how you've effectively communicated with sites and team members in previous roles. Highlight any experience you have in training or managing expectations, as this will be valuable in the interview.
✨Demonstrate Flexibility and Travel Willingness
This role requires flexibility and a willingness to travel. Be ready to discuss your past experiences that required adaptability and how you managed travel logistics while maintaining productivity. This will show your potential employer that you can handle the demands of the job.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your problem-solving skills and ability to manage multiple protocols. Think of specific situations where you successfully navigated challenges in site monitoring or recruitment, and be prepared to share these stories.
